• Merck & Co. (Rahway, NJ)
    …ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director (CRD) or Head of Site Management and Monitoring, the person is ... responsible to manage a team of 6-14 Clinical Research Associates (CRAs) and to ensure excellent study and site performance with strict adherence to local… more
    HireLifeScience (07/04/24)
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  • Merck & Co. (Rahway, NJ)
    …completed by stakeholders to facilitate an increase in efficiency and compliance for statistical/modeling analyses. -The Associate Principal Programmer will ... Job DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our companies renowned Research and Development… more
    HireLifeScience (07/03/24)
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  • Merck & Co. (Rahway, NJ)
    …Plant is a Good Manufacturing Practices (GMP) facility within the Process Research and Development (PR&D) organization which enables gain of critical internal ... to lead and support facility operations, process development activities, compliance investigations/change management, authoring of GMP documentation, and lead other… more
    HireLifeScience (07/04/24)
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  • Merck & Co. (Rahway, NJ)
    Job Description Position Description The Associate Director, Technical Operations within Global Clinical Supply (GCS) is responsible for managing all aspects of ... solid dosage forms, secondary packaging of vaccines/biologics, medical devices).Strong compliance mindset and understanding of cGMP.Demonstrated strong project leadership… more
    HireLifeScience (07/03/24)
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  • Eisai, Inc (Nutley, NJ)
    …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... make a difference. If this is your profile, we want to hear from you.The Associate Director, End User Services is responsible for the end user service delivery for… more
    HireLifeScience (06/28/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Director of Biologics Potency in Analytical Research & Development is responsible for providing strategic and technical leadership for a portion ... will be directly responsible for a team of approximately 10-15 senior and associate level scientists in Rahway, New Jersey. -The position is accountable for… more
    HireLifeScience (07/06/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary This role ... support the leader in the development and implementation of the Compliance Monitoring Program, specifically Federal healthcare laws, FDA promotional guidelines, and… more
    HireLifeScience (05/31/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.Summary The Associate ... guidelines, and policies, and meet applicable ICH and GCP standards. The Associate Director will also be responsible for the creation, management, and documentation… more
    HireLifeScience (07/05/24)
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  • Eisai, Inc (Nutley, NJ)
    …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... difference. If this is your profile, we want to hear from you.The Associate Director, Strategic Content Development, Global Medical Affairs - Alzheimer's Disease, in… more
    HireLifeScience (06/08/24)
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  • Eisai, Inc (Nutley, NJ)
    …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... difference. If this is your profile, we want to hear from you.The Associate Director, Cloud Infrastructure Architect is responsible for the design solutions and… more
    HireLifeScience (06/20/24)
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  • Merck & Co. (Rahway, NJ)
    …GMP (Good Manufacturing Practices) manufacturing facility in the Small Molecule Process Research and Development (SM PR&D) organization. The SSO pilot plant enables ... will provide hands on assistance for daily production activities while ensuring compliance with Safety & Environmental (S&E) and current Good Manufacturing Practices… more
    HireLifeScience (07/03/24)
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  • Eisai, Inc (Nutley, NJ)
    …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... and corporate goals, as well as commit to meet all compliance and reporting requirements. Requirements Bachelor's degree required; MBA preferred.Experience using… more
    HireLifeScience (06/22/24)
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  • Merck & Co. (Rahway, NJ)
    …Description Position Description: Powerhouse Chief Engineer Under the direction of the Associate Director of Engineering, The Chief Engineer is responsible for the ... deviations.The first-line supervision of twenty-four (24) licensed hourly operators. Ensures compliance with Code of Conduct, Local 68 IUOE Collective Bargaining… more
    HireLifeScience (07/04/24)
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  • Merck & Co. (Rahway, NJ)
    …of our Company's biologics pipeline.Specific Technical Responsibilities:Coordinating Bioprocess Research and Development (BPR&D) Raw materials and consumables ... lead times.Oversee shipping activities for equipment and samples, ensuring compliance with all relevant regulations and guidelines.Calibrate, conduct quality… more
    HireLifeScience (07/03/24)
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  • Merck & Co. (Rahway, NJ)
    …the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the ... include, but are not limited to:Reports to Executive Director or Associate Vice President, General MedicineDevelops worldwide product regulatory strategy to optimize… more
    HireLifeScience (07/06/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryThis is an ... and ensures that material is fully released prior to shipment to siteEnsures compliance with all domestic and foreign regulatory requirements but may seek line… more
    HireLifeScience (07/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.Summary Responsible for managing ... business teams introducing improved systems experience, cost savings, and compliance .- Stakeholder CollaborationAdvocate for the Global HRIS and collaborate with… more
    HireLifeScience (07/03/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.Summary Assist in planning ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical… more
    HireLifeScience (06/06/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary: The ... Associate Director, Field Medical Training will be responsible for...technological systems to facilitate activity/workload reporting, knowledge management and compliance management Qualifications: Successful candidates will be able to… more
    HireLifeScience (06/14/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.Summary The Associate ... alliance forecasts as well as Actuals reporting and analysis while ensuring compliance with alliance policies and procedures. Act as Alliance Committee Finance… more
    HireLifeScience (06/22/24)
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